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Low-intensity EMF induce human cryptochrome to modulate intracellular reactive oxygen species    
Ga naar overzicht berichten in: Onderzoeken

Low-intensity EMF induce human cryptochrome to modulate intracellular reactive oxygen species
zaterdag, 06 oktober 2018 - Dossier: Algemeen


Bron: journals.plos.org/plosbiology/article?id=10.1371%2Fjournal.pbio.2006229&utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+plosbiology%2FNewArticles+%28PLOS+Biology+-+New+Articles%29
PLOS Biology
2 okt. 2018

Low-intensity electromagnetic fields induce human cryptochrome to modulate intracellular reactive oxygen species

Rachel M. Sherrard , Natalie Morellini , Nathalie Jourdan, Mohamed El-Esawi, Louis-David Arthaut, Christine Niessner,
Francois Rouyer, Andre Klarsfeld, Mohamed Doulazmi, Jacques Witczak, Alain d’Harlingue, Jean Mariani, Ian Mclure,
Carlos F. Martino, Margaret Ahmad


Abstract
Exposure to man-made electromagnetic fields (EMFs), which increasingly pollute our environment, have consequences
for human health about which there is continuing ignorance and debate. Whereas there is considerable ongoing concern
about their harmful effects, magnetic fields are at the same time being applied as therapeutic tools in regenerative
medicine, oncology, orthopedics, and neurology. This paradox cannot be resolved until the cellular mechanisms underlying
such effects are identified. Here, we show by biochemical and imaging experiments that exposure of mammalian cells to
weak pulsed electromagnetic fields (PEMFs) stimulates rapid accumulation of reactive oxygen species (ROS), a potentially
toxic metabolite with multiple roles in stress response and cellular ageing. Following exposure to PEMF, cell growth is
slowed, and ROS-responsive genes are induced. These effects require the presence of cryptochrome, a putative
magnetosensor that synthesizes ROS. We conclude that modulation of intracellular ROS via cryptochromes represents
a general response to weak EMFs, which can account for either therapeutic or pathological effects depending
on exposure. Clinically, our findings provide a rationale to optimize low field magnetic stimulation for novel therapeutic
applications while warning against the possibility of harmful synergistic effects with environmental agents that further
increase intracellular ROS.

Author summary
Repetitive low-intensity magnetic stimulation has been used in the treatment of disease for over 50 years. Associated benefits
have included alleviation of depression, memory loss, and symptoms of Parkinson disease, as well as accelerated bone
and wound healing and the treatment of certain cancers, independently of surgery or drugs. However, the cellular
mechanisms underlying these effects remain unclear. Here, we demonstrate that repetitive magnetic field exposure in human
cells stimulates production of biological stress response chemicals known as reactive oxygen species (ROS). At moderate
doses, we find that reactive oxygen actively stimulates cellular repair and stress response pathways, which might account for
the observed therapeutic effects to repetitive magnetic stimulation. We further show that this response requires the function
of a well-characterized, evolutionarily conserved flavoprotein receptor known as cryptochrome, which has been
implicated in magnetic sensing in organisms ranging from plants to flies, including migratory birds. We conclude that
exposure to weak magnetic fields induces the production of ROS in human cells and that this process requires the presence
of the cryptochrome receptor.


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